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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A specific gene mutation causes a severe skin disorder in a family.

Hair color is influenced by genetics and can indicate certain health conditions.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Elephantopus scaber has many health benefits, including antibacterial, antifungal, anticancer, and antioxidant properties.

The two Eclipta alba varieties can be distinguished by their chemical differences.

Low iron levels are strongly linked to chronic hair loss in women.

Herbal hair oil helps improve hair health and prevent hair problems.

Different light affects cell functions and can help treat skin conditions.

Educators who survived COVID-19 faced physical, psychological, and social challenges but overcame them with resilience and support, highlighting the need for schools to provide better health and psychological care.

A natural hair mask was made to improve hair growth and prevent hair loss safely.

Low-level laser therapy can significantly regrow hair in alopecia areata.

Certain genetic markers may increase or decrease prostate cancer risk.

Defective protein folding due to a mutation is key in ANE syndrome.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

C-scores can help predict gain-of-function and loss-of-function mutations.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A man with severe leprosy developed painless ulcers and numbness, treated successfully with multiple drugs and vitamins.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Pretreatment methods can enhance bioactive content in lactogenic herbs.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.